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Clicking tmj causing head pressure……?
Hi All. Something I’ve not had in 33 years of RA. Have been experiencing what feels like pressure on both sides of my head and tenderness round my jaw, temples and back of neck. The pressure is the worst but it tends to come and go. My tmj’s (tempero-mandibular joints ) are tender and clicky and I can
Hi All. Something I’ve not had in 33 years of RA. Have been experiencing what feels like pressure on both sides of my head and tenderness round my jaw, temples and back of neck. The pressure is the worst but it tends to come and go. My tmj’s (tempero-mandibular joints ) are tender and clicky and I can
Amnesiac3637
in
NRAS
2 years ago
Headaches
I’m 10 months into treatment, Lupron, Ibrance and Letrazole. And I’ve had a consistent headache for two weeks. My onc ordered a brain scan. In the meantime, I’ve tried OTC pain relievers, sinus decongestants, Neurofeedback. I get some temporary relief but nothing lasting. Any suggestions?
I’m 10 months into treatment, Lupron, Ibrance and Letrazole. And I’ve had a consistent headache for two weeks. My onc ordered a brain scan. In the meantime, I’ve tried OTC pain relievers, sinus decongestants, Neurofeedback. I get some temporary relief but nothing lasting. Any suggestions?
Kiss_my_grits
in
SHARE Metastatic Breast Cancer
2 years ago
First dose of Adalimumab tried, wondering if the symptoms I got are common or not??
Upon taking the first dose, on May 26th, I used an auto injector to inject into the thigh, injection was not that bad. After about an hourish I started to get a headache, that just continued to get worse through the day, until it was pretty bad. The headache lasted pretty bad for 2 days and then mild
Upon taking the first dose, on May 26th, I used an auto injector to inject into the thigh, injection was not that bad. After about an hourish I started to get a headache, that just continued to get worse through the day, until it was pretty bad. The headache lasted pretty bad for 2 days and then mild
Jj01994
in
NRAS
2 years ago
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Don’t know where I got my brain from but…..
I’d like to send it back and get another. 13 weeks to go and I’m ever so excited, I have 3 days off work 😀 Slept like a log last night, woke at 4 cup of tea read a bit and back to sleep at 6 Willow twisted his knee walking from the bedroom to the kitchen, so he decided to walk today. To the river
I’d like to send it back and get another. 13 weeks to go and I’m ever so excited, I have 3 days off work 😀 Slept like a log last night, woke at 4 cup of tea read a bit and back to sleep at 6 Willow twisted his knee walking from the bedroom to the kitchen, so he decided to walk today. To the river
SueAppleRun
60minGraduate
in
Bridge to 10K
2 years ago
Lyrica ocular side effects and more
I am an optometrist in Colorado with severe RLS symptoms. This forum is an excellent method of sharing information on a complicated multifactorial enigma that desperately needs some solution to this pharmacologic mess. Maybe somebody can get more clues to give better relief without the nasty side effects
I am an optometrist in Colorado with severe RLS symptoms. This forum is an excellent method of sharing information on a complicated multifactorial enigma that desperately needs some solution to this pharmacologic mess. Maybe somebody can get more clues to give better relief without the nasty side effects
WelbyB
in
Restless Legs Syndrome
2 years ago
I'm back!
Hello All, I have been off this for a long time due to changes in my job and just general life changes. Has anyone (UK people) been finding that your Fibro has been kicking off more than usual? Due to the unpredictable weather (and the fact that my office is constantly cold) I have found my fibro
Hello All, I have been off this for a long time due to changes in my job and just general life changes. Has anyone (UK people) been finding that your Fibro has been kicking off more than usual? Due to the unpredictable weather (and the fact that my office is constantly cold) I have found my fibro
Maddie21
in
Fibromyalgia Action UK
2 years ago
Endometriosis, stomach inflammation, severe back, buttock, leg pain, possible bowel prolapse and other issues. Anyone else ?
Where to start? I'm 44 and believe I've had endometriosis since starting periods. Formally diagnosed late 20s. 3 lots of surgery..last one 9 years ago. I think stage 4. Have endo on my bowel. Started getting bouts of more tummy cramps and urgency to open bowels on occasions last year. Saw GP...had bloods
Where to start? I'm 44 and believe I've had endometriosis since starting periods. Formally diagnosed late 20s. 3 lots of surgery..last one 9 years ago. I think stage 4. Have endo on my bowel. Started getting bouts of more tummy cramps and urgency to open bowels on occasions last year. Saw GP...had bloods
car08500
in
Endometriosis UK
2 years ago
Ciprofloxacin Horror!
I don’t know where to start. I had been taking this drug for over a year until two days ago when I stopped it myself. I was prescribed it last April while in hospital with ARLD and alcohol hepatitis. I was very poorly and since recovered from it. My first blood tests after discharge were normal but
I don’t know where to start. I had been taking this drug for over a year until two days ago when I stopped it myself. I was prescribed it last April while in hospital with ARLD and alcohol hepatitis. I was very poorly and since recovered from it. My first blood tests after discharge were normal but
Teddy2022
in
British Liver Trust
2 years ago
Need inputs on PSA trend
My dad was diagnosed laat year with stage 4 prostate cancer and is now bedridden due to metastates to spinal cord. He is on *Zolodex injection every 3 months* for cancer. All other meds are just regular ones like hypertension, painkillers, stool softeners, vitamins etcHere are the PSA results and I
My dad was diagnosed laat year with stage 4 prostate cancer and is now bedridden due to metastates to spinal cord. He is on *Zolodex injection every 3 months* for cancer. All other meds are just regular ones like hypertension, painkillers, stool softeners, vitamins etcHere are the PSA results and I
TheMadrasMarina
in
Advanced Prostate Cancer
2 years ago
Short term use of painkillers can lead to chronic pain
Seems like a kind of evil twin of homeopathic remedies. Treatment gives you more of what you're treating. Obviously if you already have the chronic pain you must take something to relieve it, but it does call into question what longterm use does in that case. Maybe helps explain why some of us end
Seems like a kind of evil twin of homeopathic remedies. Treatment gives you more of what you're treating. Obviously if you already have the chronic pain you must take something to relieve it, but it does call into question what longterm use does in that case. Maybe helps explain why some of us end
HeronNS
in
PMRGCAuk
2 years ago
Trigeminal neuralgia and gca
However, have recently experienced acute extremely painful episodes of throbbing jaw/
facial
pain
right side of face that has woken me in night and symptoms appear to mimic trigeminal neuralgia. I did look at some of the posts on
facial
pain
.
However, have recently experienced acute extremely painful episodes of throbbing jaw/
facial
pain
right side of face that has woken me in night and symptoms appear to mimic trigeminal neuralgia. I did look at some of the posts on
facial
pain
.
Charkha
in
PMRGCAuk
3 years ago
Heart murmur symptoms and help
Hi all Can anyone give me any advice, so after seeing a doctor for my 14 year old son for something unrelated in September 2021 we were told he has a heart murmur, we have been referred to a cardiologist but still waiting for the appointment. (I’m trying to chase it without success) The letter that was
Hi all Can anyone give me any advice, so after seeing a doctor for my 14 year old son for something unrelated in September 2021 we were told he has a heart murmur, we have been referred to a cardiologist but still waiting for the appointment. (I’m trying to chase it without success) The letter that was
Helly_1000
in
British Heart Foundation
2 years ago
How i suffer with endometriosis
Hi everyone, i am val and i am 46 and i have a very painful endometriosis. I've been fine all day, til i went to my local shop and i felt the very familiar stabbing hot pain in my right groin (it's usually on the left side the most). I feel so alone with it, i don't think people in my family much care
Hi everyone, i am val and i am 46 and i have a very painful endometriosis. I've been fine all day, til i went to my local shop and i felt the very familiar stabbing hot pain in my right groin (it's usually on the left side the most). I feel so alone with it, i don't think people in my family much care
valgal76
in
Endometriosis UK
2 years ago
levo&ndt
I got some Thyroid-s ndt and I would like to take with levo but I don't know exactly how to combine them. I know that I feel more human on ndt . The last time when I took it I had more energy and a good mood but I gained weight and my knees, ankles hurt and I had to take painkillers pills. I think there's
I got some Thyroid-s ndt and I would like to take with levo but I don't know exactly how to combine them. I know that I feel more human on ndt . The last time when I took it I had more energy and a good mood but I gained weight and my knees, ankles hurt and I had to take painkillers pills. I think there's
adin
in
Thyroid UK
2 years ago
Help.
So I’ve was in hospital on Monday and discharged Wednesday was told I have a block Fallopian tube and sent homr with pain killers even though I told them I can’t manage the pain on oral morph. I was then back in hospital Thursday morning to a different hospital where they blue lighted me in an ambulance
So I’ve was in hospital on Monday and discharged Wednesday was told I have a block Fallopian tube and sent homr with pain killers even though I told them I can’t manage the pain on oral morph. I was then back in hospital Thursday morning to a different hospital where they blue lighted me in an ambulance
Adeno2020
in
Endometriosis UK
2 years ago
Nerve damage and back pain - help or advice needed
I have had 5 spinal operations, and have a fusion from L3 - S1, my last operation was about 6 years ago.I have considerable nerve damage in my legs and feet, plus constant lower back pain. It’s been steadily getting worse and now I have upper back pain, neck pain, loss of sensation in my groin, shooting
I have had 5 spinal operations, and have a fusion from L3 - S1, my last operation was about 6 years ago.I have considerable nerve damage in my legs and feet, plus constant lower back pain. It’s been steadily getting worse and now I have upper back pain, neck pain, loss of sensation in my groin, shooting
Leiimarii
in
Pain Concern
2 years ago
Tips for shoulder and back pain after endo laparoscopy?
Hello, just joined here. I had a laparoscopy yesterday and had inflamed areas in my pelvis removed. The pain in my stomach I can deal with but since waking up I’ve had the most horrendous cramping and pain in my shoulders and neck. I’ve tried all painkillers, heat and cold. Any advice?
Hello, just joined here. I had a laparoscopy yesterday and had inflamed areas in my pelvis removed. The pain in my stomach I can deal with but since waking up I’ve had the most horrendous cramping and pain in my shoulders and neck. I’ve tried all painkillers, heat and cold. Any advice?
Catrin57
in
Endometriosis UK
2 years ago
Fistula
Hi ladies, has anyone had a similar experience to me. I started 3rd line chemo carbo/ gemcitabine in mid April. Within 36 hours or so I started to have horrible abdominal pain. I went to A&E as advised by oncology helpline and they gave me pain killers. A week later I was admitted to hospital. CT scan
Hi ladies, has anyone had a similar experience to me. I started 3rd line chemo carbo/ gemcitabine in mid April. Within 36 hours or so I started to have horrible abdominal pain. I went to A&E as advised by oncology helpline and they gave me pain killers. A week later I was admitted to hospital. CT scan
Duskygem
in
My Ovacome
2 years ago
Newly diagnosed with RA
I hope I'm writing on the correct page. 2013 was diagnosed with PMR and treated with Prednisolone. went into remission in 2019. All was fine. I had Jab 1 of Covid all ok. Had jab 2 of Covid and exactly a week later all my PMR symptoms returned, November 2021. I began prednisone again 7mgs and have been
I hope I'm writing on the correct page. 2013 was diagnosed with PMR and treated with Prednisolone. went into remission in 2019. All was fine. I had Jab 1 of Covid all ok. Had jab 2 of Covid and exactly a week later all my PMR symptoms returned, November 2021. I began prednisone again 7mgs and have been
tina-shelley
in
NRAS
2 years ago
Anyone elses bones absolutely ache??
One of my recurring pains at the moment has been aching bones. It feels like the centre of all my bones (mostly arms, fingers and legs) has this deep rooted numbing pain and I'm at such a loss with it. Someone with fibromyalgia has noticed a few things about how I am and thinks I have fibro as well
One of my recurring pains at the moment has been aching bones. It feels like the centre of all my bones (mostly arms, fingers and legs) has this deep rooted numbing pain and I'm at such a loss with it. Someone with fibromyalgia has noticed a few things about how I am and thinks I have fibro as well
ArtyPal
in
Endometriosis UK
2 years ago
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